Surface Protection of Exposed Biological Tissues

ABSTRACT

The invention relates to a biodegradable barrier network comprising at least two polypeptides, one being anionic and the other one cationic. The invention also relates to applicators and kits comprising components to be used to create said biodegradable barrier network. The invention also relates to the use of said applicator or kit in therapy, such as in medicine, veterinary medicine and horticulture.

FIELD OF INVENTION

The invention relates to a biodegradable barrier network comprising twopolypeptides, one being anionic and the other one cationic. Theinvention also relates to applicators and kits comprising components tobe used to create said biodegradable barrier network. The invention alsorelates to the use of said applicator or kit in therapy, such as inmedicine, veterinary medicine and horticulture.

BACKGROUND OF INVENTION

Tissue surfaces need protection depending on the type and extent ofchemical exposure and wearing that they normally are subjected to. Allcells in the body are thus covered by a cell membrane bilayer thatmainly consists of lipids and proteins. Epithelial surfaces, whichconnect to the exterior world; the respiratory, gastrointestinal, and tosome extent also the genitourinary tracts, are exposed to a rather harshenvironment. These epithelial surfaces are further covered by a mucuslayer having viscoelastic and pronounced protecting properties. Tissuessuch as synovia and mesothelium, on the other hand, are not protected bymucus since they are not exposed to drastic condition of the samemagnitude.

In addition, the vital epithelial tissues, such as blood vessels orblood organs, are coated with mucous, serous, synovial and endothelialmembranes so that they can function independently of each other. Theperitoneal, pericardial and pleural membranes consist of a single layerof mesothelial cells, which is covered by a thin film of peritonealfluid. The components of the membranes as well as the covering layer offluid have several functions, e.g. lubrication of the enclosed organs.

The protective epithelial membrane is very thin and comprises a delicatelayer of connective tissue covered with a monolayer of mesothelial cellsand only one or a few bilayers of phospholipids. This makes the synoviaand mesothelium tissue especially vulnerable to infection and trauma.When such a membrane is exposed to a physical, chemical or microbialchallenge, many potent substances, which are harmful to the membrane,are often released in response thereto. The structure and function ofthe membrane is consequently easily destroyed in connection with trauma,ischemia, and infection. After an irritation of the stress-sensitivemembrane, e.g. only by the desiccation or abrasion of the membranesurfaces during surgery, it will rapidly be covered with a fibrin clot.Since the plasminogen activating activity (i.e. the fibrinolyticcapacity) is reduced after trauma, the fibrin clots will later on becomeorganised as fibrous adhesions, i.e. small bands or structures, by whichadjacent serous or synovial membranes adhere in an abnormal way.Surgical operations, infection or inflammation in those parts of thebody, which are coated with serous or synovial membranes, can result inadhesive inflammation regardless of the size of the affected area. Theadhesions between vital epithelial tissues are formed within the firstfew days following surgery trauma or infection and may be observed notonly in particular portions of the body but in all vital tissues. Suchadhesions between for example contact zones between intestines orbetween intestines and the abdominal wall are the result of the oftenunnoticed tissue damage as desiccation and they occur for variousreasons, including mechanical and chemical stimulation of vital tissuesaccompanying surgical manipulations, postoperative bacterial infection,inflammation or further complications.

Adhesion of vital epithelial tissues, large or small, may be observed inmost surgical fields. It has been reported that of all patientsundergoing abdominal surgery at one hospital over a four-year period,93% were found to have adhesions from previous operations. In addition,in a 10 year period there will be a need of adhesion prevention in about20% of all surgical operations, which corresponds to more than 1 millionoperations annually on each major continent.

However, the obtained postsurgical adhesions are the result of a naturalwound healing response of tissue damage occurring during surgery.Numerous factors play a role in peritoneal wound healing and thedevelopment of adhesions. Among others are peritoneal macrophages knownto have an important role in initial peritoneal repair.

Thus, while waiting after surgery for the body to produce new protectivelayers it is desired to supply the corresponding protection from theoutside to exposed epithelial surfaces in an effective way. Furthermore,it is important to prevent or reduce the infection and/or theinflammation obtained after surgery as well as the accompanying fibrinformation.

Various bioactive materials and macromolecules have been reported todecrease the extent of postoperative abdominal adhesions. Likewise, anumber of methods for limiting the formation of surgical adhesion havebeen studied with some encouraging but often ambiguous results. However,most efforts made to avoid or reduce postoperative peritoneal adhesionshave finally been abandoned. Among the methods used prevention of fibrinformation, reduction of fibrin formation, surface separation, andsurgical techniques can be mentioned.

Numerous investigations have been carried out in which barriers areplaced at a site of injury in order to prevent fibrin bridge formationbetween the injured tissue and neighboring organs. Such barriers includeresorbable materials, such as enzymatically degradable oxidizedregenerated cellulose, and slowly dissolving physiochemicallycrosslinked hydrogels of the Pluronic™ type.

Most methods of surface protection of exposed epithelial surfaces,whereby a postsurgical adhesion formation is limited, have also focusedon providing wound separation by placing a material between the tissues.In addition, several types of viscous polymer solutions such aspolyvinylpyrrolidone, sodium carboxymethyl cellulose, dextrans, andhyaluronic acid have been added before and/or at the end of surgery inorder to control the wound healing events after the occurrence of thepresumed tissue injuries. These solutions are supposed to act byincreasing the lubrication and preventing the fibrin clots from adheringto other surfaces or by mechanically separating damaged tissues whilethey heal.

The employed polymeric solutions are mainly based on the viscosity ofthe high molecular weight polymer, which is intended to increase withincreasing concentration. The polymer is often a polysaccharide as inU.S. Pat. No. 4,994,277, in which a viscoelastic gel of biodegradablexanthan gum in a water solution for preventing adhesions between vitaltissues is described. However, the major disadvantage of these polymers,when used for reducing for example peritoneal adhesions as protectivecoatings during surgery or surface separation agents after surgery, isthat they do not significantly reduce adhesions because of their shortresidence time in the peritoneal cavity. The result is that subsequentsurgeries have to be performed on the patient.

Less viscous polymer solutions have been used as a tissue protectivecoating during surgery in order to maintain the natural lubricity oftissues and organs and to protect the enclosing membrane. Precoating fortissue protection and adhesion prevention includes coating tissues atthe beginning of surgery before a significant tissue manipulation andirritation can occur and continuously throughout the operation so that aprotective coating can be maintained on the tissues.

U.S. Pat. No. 5,366,964 shows a surgical viscoelastic solution forpromoting wound healing, which is used in direct contact with cellsundergoing wound healing. The solution is intended for cell protectionand cell coating during surgery and comprises one or several polymericcomponents. Hydroxypropylmethyl cellulose and chondroitin sulphate aresupposed to lubricate the tissue, while sodium hyaluronate would provideviscoelastic properties to the solution.

Several agents of today for treating postsurgical adhesions containhyaluronic acid. For example U.S. Pat. No. 5,409,904 describes solutionswhich reduce cell loss and tissue damage intended for protectingendothelial cells during ophthalmic surgery. The compositions used arecomposed of a viscoelastic material comprising hyaluronic acid,chondroitin sulphate, modified collagen, and/or modified cellulose. InWO 9010031 a composition is described for preventing tissue adhesionafter surgery containing dextran and hyaluronic acid in which thesubstances are supposed to act synergistically. In WO 9707833 a barriermaterial for preventing surgical adhesions is shown, which comprisesbenzyl esters or covalently crosslinked derivatives of hyaluronic acid.

A hyaluronic acid based agent manufactured by Pharmacia under thetrademark Healon and originally intended as an intraocular instillationhas been found to be the most effective agent up to now. However,hyaluronic acid is isolated from cock's crests and is thus veryexpensive as well as potentially allergenic even in small quantities andeven more for large surfaces such as the peritoneum which has an area ofabout two m².

In WO 9903481 a composition for lubricating and separating tissues andbiological membranes from adjacent membranes or adjacent cells ortissues is shown, which comprises a hydrophobic polymer formed from abiologically acceptable water-soluble cationic polymer carryingcovalently bound hydrophobic groups.

Likewise, water-insoluble biocompatible compositions are shown in EP0,705,878, which comprise a polyanionic polysaccharide combined with ahydrophobic bio-absorbable polymer.

In U.S. Pat. No. 6,235,313 a variety of polymers were compared foradhesive force to mucosa surfaces. Negatively charged hydrogels, such asalginate and carboxymethyl cellulose, with exposed carboxylic groups onthe surface, were tested, as well as some positively-charged hydrogels,such as chitosan. The choice was based on the fact that most cellmembranes are actually negatively charged. However, there is still nodefinite conclusion as to what the most important property is in orderto obtain good bioadhesion to the wall of the gastrointestinal tract.For example, chitosan is considered to bind to a membrane by means ofionic interactions between positively charged amino groups on thepolymer and negatively charged sialic acid groups on the membrane. Thus,polycationic molecules, such as chitosan and polylysine, have a strongtendency to bind to exposed epithelial surfaces since these generallyhave a negative net charge.

A main drawback of both these cationic molecules is that they exhibittoxic effects. For example, polylysine is considered to act as aninhibitor of the calcium channel by producing a conformational change,thereby inhibiting transmembrane ion fluxes.

SUMMARY OF THE INVENTION

The invention relates to a new invented biodegradable barrier network,which is non-toxic, which is possible to produce at low cost,biodegradable and non-alllergenic. Such a network enables thepossibility to treat postsurgical adhesions in an efficient way.

First, the invention relates to an biodegradable barrier networkcomprising a cationic polypeptide, an anionic polypeptide and apharmaceutically acceptable carrier.

Secondly, the invention relates to an applicator comprising a cationicpolypeptide and a pharmaceutically acceptable carrier, an anionicpolypeptide and a pharmaceutically acceptable carrier, said cationic andanionic peptide being separated from each other by a separator.

Thirdly the invention relates to a kit comprising a cationic polypeptideand a pharmaceutically acceptable carrier an anionic polypeptide and apharmaceutically acceptable carrier and means for administering saidcationic and anionic polypeptide.

Finally the invention relates to a method of treating a mammal having aninjury, comprising use of the applicator or the kit according to theinvention to create the biodegradable barrier network according to theinvention.

By providing such a network, applicator and kits a new improved productwill be available on the market to be used in wound healing.

DETAILED DESCRIPTION OF THE INVENTION

Definitions

In the context of the present invention the following definitions apply:

The term “biodegradable barrier network” is intended to mean a barrier,which prevent adhesion between tissues at an injury and to provideprotection of an injured tissue against for example inflammation andinfectious agents. Additionally the barrier is degradable over timeduring the healing process of the injury.

The “network” is intended to mean a network formed between a mixture ofat least two polypeptides, where at least one is cationic and the otherone anionic.

The “same type of amino acid residue” is intended to mean that aminoacid residues in a polypeptide is for example solely H (H-H-H-H-H-H-H).

In the present context, amino acid residue names are used as defined bythe Protein DataBank (PNB) (www.pdb.org), which is based on the IUPACnomenclature (IUPAC Nomeclature and Symbolism for Amino Acids andPeptides), Eur J Biochem., 138, 9-37 (1984) together with theircorrections in Eur J Biochem., 152, 1 (1985). The term “amino acid” isintended to indicate an amino acid from the group consisting of arginine(Arg, or R), histidine (His or H), lysine (Lys or K), aspartate (Asp orD) and glutamate (Glu or E)

The Biodegradable Barrier Network

The invention relates to a biodegradable barrier network. Thebiodegradable barrier network being produced at sites of injury. Thenetwork, comprising a cationic polypeptide an anionic polypeptide and apharmaceutically acceptable carrier. The network, being formed byapplying at least one anionic and at least one cationic polypeptide insequence to a tissue. The cationic polypeptide carrier gelled in orderto focus its administration. The tissue being injured and the protectingmembrane party or totally removed. Thereby the underlying tissue beingexposed and the network will serve as protection of the exposedepithelian surfaces of a mammal, such as humans or animals.

The cationic polypetide may be selected from the group consisting ofamino acid residues R, H, K, synthetic and semisynthetic variants andmixtures thereof, such as being a poly-lysine, poly-arginine orpoly-histidine. The polypeptide may be in the L form. The polypeptidemay be a polypeptide consisting of one and the same amino acid residue,such as R-R-R-R or H-H-H-H or a mixture thereof, such as R-H-R-R-H etc.One or more synthetic or semisynthetic amino acid residues may also bepresent in the polypeptide.

The anionic polypeptide may be selected from the group consisting of theamino acid residues D, E, synthetic and semisynthetic variants, such asbeing a poly-glutamate or poly-aspartate. The polypeptide may be in theL-form. The polypeptide may be a polypeptide consisting of one and thesame amino acid residue, such as D-D-D-D or E-E-E-E or a mixturethereof, such as D-D-E-D-E. One or more synthetic or semisynthetic aminoacid residues may also be present in the polypeptide.

The length of the polypeptides may be the same or different, dependingon where the biodegradable barrier network should be formed, i.e.,depending on which tissue it should be applied to. The size may be atleast 5.000 Da, such as between about 5.000 to about 50.000 Da. Examplesare 6.000, 7.000, 8.000, 10.000, 15.000, 20.000, 30.000, 40.000 andmixtures thereof.

Additionally, at least one of the above mentioned polypeptides may belinked to at least one different neutral amino acid residue, otherpeptides or other substances, such as a substance which cleans theinjuried surfaces, provides antioxidants, modulates apoptosis, promoteshealing, inhibits fibrogenesis and tumour growth, controls bleeding,inhibits inflammation, increases stability or protects againstinfection. Examples are antimicrobial agents, antiinflammatory agents,cleaning agents, antioxidants, apoptosis modulators, healing agents,fibrogenesis inhibitors, antitumor agents and antibleeding agents.

Accordingly the polypeptides may be modified by amidation,esterification, acylation, acetylation, PEGylation or alkylation

The above mentioned network may also comprise a pharmaceuticalacceptable diluent or buffer. “Pharmaceutically acceptable carrier”means a non-toxic substance that does not interfere with theeffectiveness of the surface protection activity of the polypeptides.Such acceptable buffers or diluents are well-known in the art (seeRemington's Pharmaceutical Sciences 18^(th) edition, A. R Gennaro, Ed.,Mack Publishing Company (1990).

The term “buffer” is intended to mean an aqueous solution containing anacid-base mixture with the purpose of stabilising pH. Examples ofbuffers are Trizma, Bicine, Tricine, MOPS, MOPSO, MOBS, Tris, Hepes,HEPBS, MES, phosphate, carbonate, acetate, citrate, glycolate, lactate,borate, ACES, ADA, tartrate, AMP, AMPD, AMPSO, BES, CABS, cacodylate,CHES, DIPSO, EPPS, ethanolamine, glycine, HEPPSO, imidazole,imidazolelactic acid, PIPES, SSC, SSPE, POPSO, TAPS, TABS, TAPSO, TES,tricine.

The term “diluent” is intended to mean an aqueous or non-aqueoussolution with the purpose of diluting the peptide in the pharmaceuticalpreparation. The diluent may be one or more of saline, water,polyethylene glycol, propylene glycol, ethanol or oils (such assafflower oil, corn oil, peanut oil, cottonseed oil or sesame oil).

The invented network may also comprises one or more therapeutic agentsuch as an antimicrobial, antiinflammatory agent, substances whichcleans the injuried surfaces, provides antioxidants, modulatesapoptosis, promotes healing, inhibits inhibits fibrogenesis and tumourgrowth or controls bleeding.

Examples of therapeutic agents are penicillins, ephalosporins,carbacephems, tetracyclines, macrolides, iodine, silver, copper,clorhexidine, acetylsalicylic acid and examples of cleaning substancesare proteolytic enzymes.

Examples of agents having antioxidant activity are various vitamins,glutathione, folic acid, curcumin, resveratrol, epigallocathechin,anthocyanidins and numerous other agents.

Examples of agents which modulates apoptosis, inhibits fibrogenesis andtumour growth are glucocorticosteroids, insulin, dexamethasone,carotenoids, linoleic and conjugated-linoleic acids, melatonin,isothiocyanates, shikonin, solamargine, perifosine, deoxynivalenol,carboxyamido-triazole (CAI), histone deacetylase inhibitors and numerousother agents.

Examples of agents which promotes healing are various growth factors,insulin, vitamin E, retinoic acid, herbal components and numerous otheragents and examples of agents which controls bleeding arenorepinephrine, gelatin, collagen, oxidized cellulose and numerous otheragents.

The above mentioned polypeptide can be synthesised by standard chemicalmethods including synthesis by automated procedure. In general, peptideanalogues are synthesised based on the standard solid-phase Fmocprotection strategy with HATU(N-[DIMETHYLAMINO-1H-1.2.3.-TRIAZOLO[4,5-B]PYRIDIN-1-YLMETHYLELE]-N-METHYLMETHANAMINIUM HEXAFLUOROPHOSPHATEN-OXIDE) as the coupling agent or other coupling agents such asHOAt-1-HYDROXY-7-AZABENZOTRIAZOLE. The peptide is cleaved from thesolid-phase resin with trifluoroacetic acid containing appropriatescavengers, which also protects side chain functional groups. Crudepeptide is further purified using preparative reversed-phasechromatography. Other purification methods, such as partitionchromatography, gel filtration, gel electrophoresis, or ion-exchangechromatography may be used. Other synthesis techniques, known in theart, such as the tBoc protection strategy, or use of different couplingreagents or the like can be employed to produce equivalent peptides.

An Applicator or Kit of the Invention

Additiaonally, the invention relates to an applicator comprising acationic polypeptide and a pharmaceuticaly acceptible carrier, ananionic polypeptide and a pharmaceutically acceptable carrier, saidcationic and anionic polypeptide being separated from each other by aseparator. The polypeptides being as defined above and the solution is apharmaceutically acceptable solution as defined above.

The applicator may be syringes, one or two component sprays, nebulators,plasters, catheters, adhesives, implants and bandages.

The separator separating the anionic and the cationic polypeptide priorto that they are applied to an injured tissue may be any separator aslong as it is non-toxic and does not influence the effect of thepolypeptides. The separator may be biodegradable. The main function of aseparating layer between the two polypeptide solutions is to wash outall of the cationic peptide before administration of the polyanionic oneand to avoid precipitation already in the applicator. It shouldtherefore only consist of distilled water or the buffer used in solutionof the polypeptides. However, this water solution should not dilute thepolypeptide solutions and should therefore not be administrated on thefirst applied cationic polypeptide. The separator may be a gelled stateof the aqueous solution. Additionally the separator may be a membrane.

Additionally, the applicator may comprise one or more therapeuticagents, such as those defined above. The agents, being (separated fromthe two polypeptides or) mixed with one or both of the polypeptides.

The therapeutic agent may be selected from the group consisting ofpenicillin, cephalosporin, carbacephems, tetracyclines, macrolides,iodine, silver, copper, clorhexidine and antiinflammatory agents such asacetylsalicylic acid.

Accordingly the invention relates to a kit comprising a cationicpolypeptide and a pharmaceutically acceptable carrier, an anionicpolypeptide and a pharmaceutically acceptable carrier and means foradministering said cationic and anionic polypeptide. The polypeptidesbeing as defined above.

The means may be selected from the group consisting of syringes, sprays,plasters, catheter, adhesives, implant and bandages.

Additionally the kit may comprise one or more therapeutic agent such asantimicrobial and antiinflammatory agents. Other suitable therapeuticagents are those defined above. The therapeutic agent is selected fromthe group consisting of penicillin, cephalosporin, carbacephems,tetracyclines, macrolides, iodine, silver, copper, clorhexidine andacetylsalicylic acid.

The therapeutic agent in the applicator or kit described above may beseparated from the two polypeptides or mixed with one or both of thepolypeptides.

The applicator and/or the kit as described above may be used in therapy,such as in medicine, veterinary and horticulture.

Finally the invention relates to a method of treating a mammal having aninjury, comprising use of the applicator and/or the kit as describedabove, creating the disclosed network. Examples of areas in which theinvention can be useful includes ophtalmic bulb injuries and infections,nasal wounds, injuries and infections, skin injuries and infections, sunburns, thermic skin injuries/burns, bed sores, chronic leg ulcers,vaginal wounds, urinary bladder inflammation, oesophageal and stomachulcers, inflammation and ulcers of the intestine, inflammations andserosal injuries of joints, cut surfaces or injuries to solid organssuch as lung, liver and spleen, bone injuries, peritoneal defects andinflammation.

EXAMPLES

The invention will now be further described and illustrated by referenceto the following examples. It should be noted, however, that theseexamples should not be considered as limiting the invention in any way.

Example 1 Adhesion Prevention.

A reproducible and standardized rat and rabbit model was adopted. Fortyeight female MRI mice weighing about 25-30 g were used to induce theadhesions and forty two for further tests. The animals were kept understandardized conditions and had free access to pellet and tap water.

Anesthesia was induced by ketamine 150 mg/kg (Ketalar, Parke Davis) andzylazine 7.5 mg/kg (Rompun, Bayer Sverige AB) intramuscular injection.After disinfection, a 25 mm long midline laparotomy was performed. Bothperitoneal surfaces of the lateral abdominal wall were exposed, and 2×15mm long sharp incisions were performed at the same distance from themidline, including the muscles. The wounds were immediately closed with2×4 single sutures at equal distances by using 5.0 polypropylene(Prolene, Ethicon, Johnson & Johnson). The midline laparotomy was closedin two layers with a continuous 5.0 polypropylene suture. At theevaluation time an overdose of anesthetic was administered, the abdomenwas totally opened through a U-shaped incision with its base to theright. The lengths of the adhesions were measured on both sides using ametal caliper, and data was expressed as percent wounds covered byadhesions.

Aqueous solutions of 0.5% poly-L-glutamate, and poly-L-lysine werefreshly made on the day of the experiment and stored in refrigator untilused. FITZ-labeled polylysine was mixed with polylysine in a proportionof 1:10 (wt). All chemicals and cell culture substrates were purchasedfrom Sigma-Aldrich, St Louis, USA; fluorescent microparticles (Nile BlueLabeled) were bought from Microparticles GmbH., (Berlin, Germany).

The animals were divided randomly into 4 groups based on the treatmentand the evaluation time. The control groups were intraperitoneallyinjected with 2 ml physiologic sodium chlorine solution. Two treatmentgroups received 1 ml poly-L-lysine solution and 5 min later 1 mlpoly-L-glutamate solution. One of the control and treatment groups (2×14animals) was sacrificed one week after surgery and the lengths of theadhesions were calculated. The remaining two groups (2×10 animals) werekept for four weeks before they underwent the evaluation process.

The Kruskal Wallis test was used to determine the difference in adhesionamount among the different treated groups and the Mann Whitney U testwas used to compare the individual groups.

A significant decrease in adhesion development was detected both oneweek and one month after the peritoneal challenge (**p≦0.001) comparedto the corresponding controls (Mann-Whitney U test) . A marked (22%)though not significant (p=0.235) decrease was obtained after one monthbetween the control groups, while there were no difference between thetreated groups by that time.

No adhesions were found which were related to a heavy compound depositin different locations from the wound itself. After 24 h, the animalsthat had been given both poly-L-lysine and poly-L-glutamate exhibited amassive protecting layer over the periotoneal wound, and thin film atthe rest of peritoneal surface. However the FITZ-labeled compound wasonly visible in the wound one day later and was detectable both over andinside the wound. The deposit was gradually rebuilt until the end of the6 day observation period.

Example 2 Phagocytosis and Particle Ingestion Index.

The time course of the phagocyte function was tested in vitro onperitoneal resident macrophages from mice after 0.5 h, 1 h, 2 h, 3 h, 4h, 5 h, 6 h, 8 h, 10 h, 12 h, 16 h, and 24 h incubation withpoly-L-lysine+poly-L-glutamate (40 μg/ml) and/or fluorescent particles(1 μm).

Macrophage samples were taken by abdominal lavage with 10 ml ice coldDMEM-solution. The samples in medium were immediately centrifuged at1200 rpm for 10 min. The cells were resuspended in DMEM containing 10%FBS and penicillin/streptomycin and then plated on 48 wells cell cultureplates; 5×10⁵ cells in each well. After 1.5 h non-adherent cells werewashed away, particles (100/cell) together with test drugs(poly-L-lysine+poly-L-glutamate) were added in a dose of 40 μg/ml to12×5 wells, and particles only were added to the remaining 12×5 wells.More-over negative controls were performed at each time point. The cellswere incubated (37° C., 5% CO₂) and detached and fixed at the evaluationtime by using 250 μl mM EDTA and an equal volume of 2% paraformaldehyde.FACS analysis (FACScan, Becton Dickinson, San Jose, Calif.) was made,when cell size (forward scatter, FSC), granularity (side scatter, SSC)and fluorescence intensity (in FL3 channels) were recorded of 1.5×10⁴cells in each measurement. In manually defined gates the ratiophagocyting cells/total macrophages was expressed in percent as mean ofdata from five wells at each time and treatment group (control andpoly-L-lysine+poly-L-glutamate).

The non-treated cells incorporated more particles. Thus, the maximumplateau (median) level of their fluorescence intensity (FL3) and SSC wasset as 100%. All measurements were expressed as the median percentage ofthe plateau level and termed particle ingestion index, since it refersto the amount of particles ingested.

The Mann Whitney U test was used to check the plateau of phagocytosisand the Wilcoxon Signed Ranks test was used to test the difference inthe phagocytosis and particle ingestion index between the treatmentpairs (control and poly-L-lysine+poly-L-glutamate, respectively).

While the phagocytosis index of the non-treated macrophages reached theplateau of phagocytosis about 5 h (the difference between 4 and 5 hdecreased below the insignificant level, p=1), the treated populationrequired 8 h for the same effect. (The difference between 8 and 10 h wasinsignificant, p=0.058). A low but significant (p=0.043) difference wasobtained in the phagocytosis index after 24 h (97.3% and 94.3%,respectively).

The time course for the ingestion index, which refers to the number ofparticles phagocytosed by macrophages became significant between 1 and 2h (p=0.008). The control cell population reached the plateau between 16and 24 h (insignificant difference between the index at 12 and 24 h(p=0.841) while the treated cell population did not reach the plateau atall during the first 24 h studied. Furthermore, the number of ingestedparticles were significantly lower in the treated group at all times(p=0.043).

Flow cytometry verified that macrophages phagocyte the test compoundparticles, which resulted in significant cell growth and largephagocytic vacuoles.

Example 3 Transmission Electron Microscopy.

Peritoneal macrophages were harvested from two healthy non-treatedanimals as described above and plated on cell culture plates (Thermanox,Naperville, Ill., USA). The cells were washed away after 1.5 h andpoly-L-lysine+poly-L-glutamate (40 μg/ml) in supplemented DMEM solutionwere added in sequence followed by a 24 h incubation. The incubationmedium was removed and the cells were fixed in 2.5% phosphate bufferedglutaraldehyde was followed by rinsing in Milloning's phosphatesolution. Samples were postfixed in 1% osmium tetroxide and subsequentlydehydrated with graded series of ethanol, which was followed byembedding in Araldite 502 kit. Vertical sections were obtained with adiamond knife and stained with uranyl acetate and lead citrate in a LKBUltrastainer. Samples were examined in a JEOL 1200 EX transmissionelectron microscope (TEM).

Electron microscopy verified that macrophages phagocyte the testcompound particles, resulted in significant cell growth, and largephagocytic vacuoles.

Example 4 Scanning Electron Microscopy.

Peritoneal swabs and wounds were taken from eight treated (4) andnon-treated (4) animals after one and seven days of surgery and cellcultures were conducted as above. The samples were fixed in 2.5%phosphate buffered glutaraldehyde at room temperature and thenpost-fixed in 1% OSO₄. The samples were dehydrated in acetone, criticalpoint dried and sputter-coated with gold before being studied in a LEO420 electron microscope.

SEM data showed that mesothelial cells covered the compound surface fromthe first day.

Example 5 Histology.

Eight animals were opened and then injected intraperitoneally withpoly-L-lysine+poly-L-glutamate. At the postoperative first, second,third, and sixth days, two animals were sacrificed and the wounds wereexcised. They were rapidly frozen and embedded, and the block obtainedwas immediately cut into slices of 7 μm. The slices were allowed to dryin dark for 30 min at room temperature and were then stained with 100μg/l 4′6′-diamino-2-phenylindole hydrochloride (DAPI) solution for 10min. Fluorescent microscopy was performed with both a FITZ and a DAPIfilter, and images were digitally merged (OpenLab, Improvosion). Macrophoto was made about the excised wounds by using trans-illumination,mixed ambient room light, and UV illumination.

The histological studies showed that the added material was present inthe wound from the first day. Furthermore, more and more cells weredetected for each day until the matrix was completely rebuilt.

Example 6 Biodegradation.

Healthy non-operated animals were treated intraperitoneally as inExample 1 and sacrificed after two months.

No visible remains of poly-L-lysine and poly-L-glutamate could bedetected. The biodegradability is supported by findings that at onemonth's follow up the same results were obtained by using a double doseof poly-L-lysine+poly-L-glutamate, although that caused some additionaladhesions related to the compound at evaluation on the 7^(th) day.

Example 7 Biodegradation.

Aqueous solutions of 1% and 2% lysozyme, poly-L-glutamate,poly-L-lysine, and poly-L-glutamate, and 0.25% of hyaluronic acid werefreshly made. Solutions of lysozyme, polyglutamate,lysozyme+polyglutamate and polylysine+polyglutamate were thenadministered to animals as in Example 1.

The extent of abdominal adhesions one week after surgery significantlydecreased in the four treated groups (p≦0.001) as compared to controls.However, no significant change in response was obtained with hyaluronicacid (p=0.264). The combinations poly-L-lysine/lysozyme seemed to resultin an insoluble product.

Example 8 Effect of Poly-L-Lysine Alone.

An aqueous solution of 0.5% poly-L-lysine was freshly made andadministered to animals as in Example 1.

Such an administration of poly-L-lysine alone resulted in convulsionsand death within 30 min, i.e. before they woke up from the anesthesia.The symptoms seemed to be related to the effect of opening calciumchannels, plasma Ca⁺⁺ levels being rapidly decreased.

Outlay of the Experimental Procedure

-   -   a. Standard thermic injuries were produced on the two sides of        the back of ten mice. One wound was treated with the        composition, the other served as control. Reduced rate of        infection, faster healing and less sequelae were seen in the        treated wounds.    -   b. One cm long incisions were done on each side of the back of        ten rats. One incision was filled with the composition, the        other served as control. Uneventful and faster healing was        observed of the treated wound.    -   c. Standard incisions were done in both the liver and spleen of        ten rats. Additional ten rats served as controls. The amount of        bleading was significantly reduced in the treated animals. The        treatment glued together the defect, which resulted in a faster        healing and less sequelae.    -   d. Colonic mucosa inflammation and wounds were induced in rats        by several methods such as acetic acid infusion, methotrexate        and dextran sulphate. The inflammatory surfaces and wounds were        “painted” with the composition. Reduced inflammation and        enhanced healing was observed.    -   e. Human nasal mucosa wounds and infections were treated with        the composition. A fast cleansing of the wounds and healing was        observed.    -   f. Human bed sores were treated by the composition. A fast        cleansing of the infected and necrotic surfaces was observed.        The treatment was repeated over a longer period of time.    -   g. Human chronic leg ulcers were treated by the composition, A        fast cleansing of the infected and necrotic surfaces was        observed. The treatment was repeated over a longer period of        time.

1. An biodegradable barrier network, comprising: a) a cationicpolypeptide, b) an anionic polypeptide and c) a pharmaceuticallyacceptable carrier.
 2. The biodegradable barrier network according toclaim 1, wherein a) is selected from the group consisting of amino acidresidues R, H, K, synthetic and semisynthetic variants and mixturesthereof.
 3. The biodegradable barrier network according to claim 2,wherein b) is selected from the group consisting of the amino acidresidues D, E, synthetic and semisynthetic variants and mixturesthereof.
 4. The biodegradable barrier network according to claim 1,wherein the amino acid residues within at least one of the polypeptidescomprise amino acid residues of the same type.
 5. The biodegradablebarrier, network according to claim 1, wherein at least one of thepolypeptides is linked to one or more amino acid residues, otherpeptides or other substances.
 6. The biodegradable barrier networkiaccording to claim 1, wherein at least one of the peptides is modifiedby amidation, esterification, acylation, PEGylation or alkylation. 7.The biodegradable network according to claim 1, wherein the peptideshave a size of at least 5,000 Da, such as from about 5.000 to about50.000 Da.
 8. The biodegradable barrier network according to claim 1,wherein the biodegradable network comprises a pharmaceutical acceptablecarrier, such as a diluent or buffer.
 9. The biodegradable barriernetwork according to claim 1, wherein the biodegradable networkicomprises a therapeutic agent such as antimicrobial agents,antiinflammatory agents, cleaning agents, antioxidants, apoptosismodulators, healing agents, fibrogenesis inhibitors, antitumor agentsand antibleeding agents.
 10. The biodegradable barrier network accordingto claim 9, wherein the therapeutic agent is selected from the groupcomprising of penicillins, cephalosporins, carbacephems, tetracyclines,macrolides, iodine, silver, copper, clorhexidine, acetylsalicylic acid,proteolytic enzymes, vitamins, glutathione, folic acid, curcumin,resveratrol, anthocyanidins, glucocorticosteroids, insulin,dexamethasone, carotenoids, linoleic and conjugated-linoleic acids,melatonin, isothiocyanates, shikonin, solamargine, perifosine,deoxynivalenol, carboxyamido-triazole (CAI), histone deacetylaseinhibitors, growth factors, insulin, vitamin E, retinoic acid, herbalcomponents norepinephrine, gelatin, collagen and oxidized cellulose. 11.An applicator comprising: a) a cationic polypeptide and apharmaceutically acceptable carrier; b) an anionic polypeptide and apharmaceutically acceptable carrier; said cationic polypeptide andanionic polypeptide being separated from each other by a separator. 12.The applicator according to claim 11, wherein the applicator is selectedfrom the group comprising of syringes, one or multi-component sprays,nebulators, plasters, catheters, adhesives, implants and bandages. 13.The applicator according to claim 11, wherein the separator is a gelledaqueous solution or a membrane.
 14. (canceled)
 15. A kit comprising a) acationic polypeptide and a pharmaceutically acceptable carrier b) ananionic polypeptide and a pharmaceutically acceptable carrier and c)means for administering said cationic and anionic polypeptide. 16.(canceled)
 17. The kit according claim 15, wherein the means is selectedfrom the group comprising of syringes, plasters, catheters, adhesives,implants, bandages, one or multi-component sprays, and nebulators. 18.The applicator according to claim 11, comprising a therapeutic agentsuch as antimicrobial agents antiinflammatory agents, cleaning agents,antioxidants, apoptosis modulators, healing agents, fibrogenesisinhibitors, antitumor agents and antibleeding agents.
 19. The applicatoraccording to claim 18, wherein the therapeutic agent is selected fromthe group comprising of penicillins, cephalosporins, carbacephems,tetracyclines, macrolides, iodine, silver, copper, clorhexidine,acetylsalicylic acid, proteolytic enzymes, vitamins, glutathione, folicacid, curcumin, resveratrol, epigallocathechin, anthocyanidins,glucocorticosteroids, insulin, dexamethasone, carotenoids, linoleic andconjugated-linoleic acids, melatonin, isothiocyanates, shikonin,solamargine, perifosine, deoxynivalenol, carboxyamidotriazole (CAI),histone deacetylase inhibitors, growth factors, insulin, vitamin E,retinoic acid, herbal components norepinephrine, gelatin, collagen andoxidized cellulose.
 20. The applicator according to claim 18, whereinthe therapeutic agent is separated from the two polypeptides or mixedwith one or both of the polypeptides.
 21. (canceled)
 22. A method oftreating a mammal having an injury, comprising use of the applicatoraccording to claim 11 for creating the biodegradable barrier network.